# Control of reproductive aging by germline stem cells

> **NIH NIH F31** · WASHINGTON UNIVERSITY · 2024 · $34,926

## Abstract

Project Summary/Abstract
Adult stem cell exhaustion is a hallmark of aging. However, mechanisms of stem cell exhaustion during aging
are largely unknown, and there are no therapies that can delay stem cell aging in humans. C. elegans is a
premier model organism for studying aging; adult animals are short lived and only contain one stem cell pool,
the germline stem cells that generate eggs and sperm. Extensive developmental studies have provided a rich
description of the molecular and cellular events that control these stem cells in young animals. My goal is to
understand stem cell exhaustion, and my strategy is to exploit the experimental power of C. elegans and the
detailed knowledge of stem cell development to elucidate stem cell aging. The somatic distal tip cell (DTC) serves
as the stem cell niche by expressing the Notch pathway ligands LAG-2 and APX-1, which bind and activate the
GLP-1/Notch receptor in the stem cells. Notch signaling pathways are conserved during evolution and have been
repeatedly implicated in regulating stem cells in mammals, suggesting the niche/stem cell system in worms is
likely to be broadly relevant. Elucidating the regulatory logic of this system will advance the fields of
reproductive aging and stem cell exhaustion. Preliminary results from our lab demonstrate that the number
and activity of germline stem cells decline rapidly and progressively with age. Based on these results, I propose
two innovative hypotheses. (1) An age-related decline in Notch signaling from the DTC niche causes stem cell
exhaustion. (2) Neuronal TGF-β signaling mediates the activity of the DTC niche and contributes to the age-
related decline of adult stem cells in the germline. To test these hypotheses, I propose two specific aims. Aim
1: Elucidate mechanisms of Notch pathway regulation during adult stem cell aging in the germline. I will
monitor LAG-2 ligand expression in the DTC niche during aging and analyze LAG-2 ligand and Notch receptor
function. The results will rigorously test my hypothesis by establishing how LAG-2 ligand expression is regulated
during aging and whether LAG-2 ligand and/or GLP-1/Notch receptor are sufficient to sustain stem cell activity
during aging. Aim 2: Determine how sensory neurons regulate the DTC niche to mediate germline stem
cell aging. I will analyze the DAF-3 binding site in the lag-2 promoter, and the DAF-3 and DAF-5 transcription
factors that are the effectors of TGF-β signaling. I will examine multiple levels of organization including protein
expression, stem cell dynamics, and progeny production. The results will establish how neuronal signals control
the niche and stem cells during aging. The mechanisms of stem cell exhaustion remain mysterious, and these
experiments will advance the field by determining the contributions of neurons, the niche, and the stem cells
themselves. The results will establish a foundation of knowledge that may stimulate innovative approaches to
preserve stem cell function ...

## Key facts

- **NIH application ID:** 10915433
- **Project number:** 5F31AG084277-02
- **Recipient organization:** WASHINGTON UNIVERSITY
- **Principal Investigator:** Aaron Marcus Anderson
- **Activity code:** F31 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $34,926
- **Award type:** 5
- **Project period:** 2023-08-01 → 2026-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10915433

## Citation

> US National Institutes of Health, RePORTER application 10915433, Control of reproductive aging by germline stem cells (5F31AG084277-02). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10915433. Licensed CC0.

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